Coordinates and tracks submissions to EU Notified Bodies under MDR for DePuy Synthes, acting as the primary point of contact for project planning with Notified Body counterparts. Develops detailed project plans, timelines and status reports, manages risks and mitigation, and liaises with business units and EU regulatory personnel to expedite approvals. Also supports continuous improvement of project management and regulatory processes.
Coordinates and tracks Technical Documentation and Change Notification submissions to EU Notified Bodies under MDR, acting as the primary point of contact for project planning with Notified Body counterparts. Develops detailed project plans, timelines and status reports, manages risks and mitigation, and liaises with business units and regulatory agency personnel to expedite approvals. Also supports continuous improvement of project management practices.
Drives adoption of aortic therapies across Western Europe, translating regional strategy into field-ready market development plans and leading product launches. Also leads Digital Solutions initiatives, partnering with regional and global stakeholders to drive implementation and business impact. Requires cross-functional influence in a matrix organisation, with aortic or vascular experience preferred.
Leads global cross-functional teams to design, implement and commercialise digital, electro-mechanical and robotic medical devices, managing multiple complex hardware and embedded software programmes from initiation through delivery. Involves risk management, requirements planning and reporting to executive leaders, using waterfall, Scrum and Agile methods in a highly regulated, safety-critical environment.
Field-based role owning a strategic orthopaedic revision territory from the M1 corridor to the East of England, partnering with surgeons and theatre teams on complex cases. Supports procedures in theatre, leads product introductions and tenders, and drives adoption of an innovative portfolio including robotics, working alongside Account and Area Business Managers.
Field-based role owning a strategic orthopaedic revision territory from the M1 corridor to the East of England, supporting complex surgical cases in theatre and building relationships with surgeons and theatre teams. Combines clinical expertise with commercial account planning, tenders and product introductions, including advanced technologies such as robotics.
Consultative field sales role promoting vascular access and oncology medical devices to NHS and private healthcare customers across the M25 region. Roughly 80% new business generation and 20% account development, including quotations, equipment demonstrations, and attendance at fairs and congresses, with full training and mentoring provided.
Consultative field sales role promoting vascular access and oncology medical devices to NHS and private healthcare customers across the M25 region, with 80% new business generation and 20% account development. Involves working in operating room environments, preparing quotations and demonstrating equipment, plus attending fairs and congresses. Full training and mentoring is provided for entrants from graduate, clinical or B2B sales backgrounds.
Field-based role supporting chemistry and immunoassay analysers for laboratories across South Wales, with occasional UK travel. Involves installation support, end-user training, troubleshooting, workflow optimisation and software updates, with additional exposure to Molecular and Tissue Diagnostics platforms. Customer-facing, working within a central application team.
Coordinate product development projects from sourcing and concept evaluation through to launch, sourcing materials and prototypes for testing. Maintain product and raw material specifications, work with suppliers on technical and quality requirements, and support cost-effective manufacturing. Provide technical product information to sales and marketing teams while ensuring quality, health and safety and regulatory compliance.
Leads customer-facing Radiology Informatics programs covering PACS, RIS and enterprise imaging, managing software implementations from order signature through go-live and handover. Runs large cross-functional projects with budgets typically over £1M, handling scope, risk, budget and stakeholder governance. Field-based across the UK, Ireland and Nordics, working from home with around 60% travel to customer sites.
Independently manage end-to-end clinical data management for one or more studies, from CRF and database design through to final study closure. Collaborate with Biostats, Data Science and Clinical teams to define data specifications, resolve complex data issues using risk-based monitoring, and oversee third-party vendors to meet regulatory and quality expectations.
Provide regulatory support across a Cambridge product development business, guiding multidisciplinary engineering and science teams on compliance with ISO 9001, ISO 13485 and FDA 21 CFR 820. Monitor international regulatory changes, support external audits and contribute to quality management system improvements across medical and non-medical projects.
Mechanical engineer consultant bridging client ambition and technical delivery for drug delivery devices and combination products. Involves concept creation, analysis, modelling, detailed design, rapid prototyping and hands-on experimental work from lab to pilot scale, plus scoping, proposals and client relationship building.
Provide regulatory support across a product development organisation, working with engineers and scientists to align projects with global requirements. Maintain and improve the QMS, apply ISO 9001, ISO 13485 and FDA 21 CFR 820, monitor regulatory changes, and support external audits.
